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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 215897Generated: October 25, 2026

Hydrochloric Acid → 1-[4-(5-Cyanoindol-3-yl)butyl]-4-(2-carbamoyl-benzofuran-5-yl)-piperazine dihydrochloride

https://huagongshe.com/reaction/215897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantVilazodoneHCID 6918314—
SolventTetrahydrofuranHCID 8028—
Product1-[4-(5-Cyanoindol-3-yl)butyl]-4-(2-carbamoyl-benzofuran-5-yl)-piperazine dihydrochlorideHCID 67300892—

Reaction Steps

3 g of 1-[4-(5-cyanoindol-3-yl)butyl]-4-(2-carbamoyl-benzofuran-5-yl)-piperazine is dissolved in 100 ml of tetrahydrofuran and 10 ml of 2N or concentrated hydrochloric acid. After stirring for 2 to 3 minutes suction filtration of the precipitated crystals is effected. Drying in vacuo at room temperature to constant weight leads to 1-[4-(5-cyanoindol-3-yl)butyl]-4-(2-carbamoyl-benzofuran-5-yl)-piperazine dihydrochloride of Form XIII which present the characteristic x-ray diffraction spectrum of FIG. 25.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193195B2
Source datasetuspto-grants-2012_06
ORD IDord-a4122d9f706b492785cb0ae4cb016701
Source noteuspto-grants-2012_06